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List of NDC API details of CLOMIPHENE-CITRATE Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Enclomiphene Citrate
POWDER (1kg/kg)
BULK INGREDIENT
71052-506
2022-05-04
2024-12-31
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Clomiphene Citrate
POWDER (50g/50g)
BULK INGREDIENT
71052-338
2019-08-22
2024-12-31
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Looking for 7619-53-6 / Clomiphene Citrate API manufacturers, exporters & distributors?

Clomiphene Citrate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Clomiphene Citrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Clomiphene Citrate manufacturer or Clomiphene Citrate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clomiphene Citrate manufacturer or Clomiphene Citrate supplier.

PharmaCompass also assists you with knowing the Clomiphene Citrate API Price utilized in the formulation of products. Clomiphene Citrate API Price is not always fixed or binding as the Clomiphene Citrate Price is obtained through a variety of data sources. The Clomiphene Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Clomiphene Citrate

Synonyms

50-41-9, Zuclomiphene citrate, Cis-clomiphene citrate, Clomid, Zuclomid, Clomiphene a citrate

Cas Number

7619-53-6

Unique Ingredient Identifier (UNII)

UY5X264QZV

About Clomiphene Citrate

A triphenyl ethylene stilbene derivative which is an estrogen agonist or antagonist depending on the target tissue. Note that ENCLOMIPHENE and ZUCLOMIPHENE are the (E) and (Z) isomers of Clomiphene respectively.

CLOMIPHENE-CITRATE Manufacturers

A CLOMIPHENE-CITRATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CLOMIPHENE-CITRATE, including repackagers and relabelers. The FDA regulates CLOMIPHENE-CITRATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CLOMIPHENE-CITRATE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of CLOMIPHENE-CITRATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

CLOMIPHENE-CITRATE Suppliers

A CLOMIPHENE-CITRATE supplier is an individual or a company that provides CLOMIPHENE-CITRATE active pharmaceutical ingredient (API) or CLOMIPHENE-CITRATE finished formulations upon request. The CLOMIPHENE-CITRATE suppliers may include CLOMIPHENE-CITRATE API manufacturers, exporters, distributors and traders.

click here to find a list of CLOMIPHENE-CITRATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

CLOMIPHENE-CITRATE NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing CLOMIPHENE-CITRATE as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for CLOMIPHENE-CITRATE API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture CLOMIPHENE-CITRATE as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain CLOMIPHENE-CITRATE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a CLOMIPHENE-CITRATE NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of CLOMIPHENE-CITRATE suppliers with NDC on PharmaCompass.

CLOMIPHENE-CITRATE Manufacturers | Traders | Suppliers

CLOMIPHENE-CITRATE Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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